Job Description Responsible for in process Quality Assurance activities Responsible for In process Quality Assurance checks during Manufacturing, packing operations. Responsible for line clearance of manufacturing, Packing and dispensing activities. Responsible for assurance of cleaning, sterilization and aseptic manipulations of components Responsible for Sampling of Cleaning Validation & Compilation of the records. Responsible for sampling and coordination during validation studies (process / cleaning validation). Responsible for routine monitoring of Manufacturing Areas. Responsible for Review of Batch Manufacturing Record (BMR) & Batch Packing Records (BPRs). Responsible for the routine GMP Inspection & review of Quality Records of other departments. Responsible for monitoring in Aseptic process simulation study. Responsible for Preparation and Compilation of Media Fill Protocol , Report Involve in Initiation of Change Control ,Deviation and Participate in Failure Investigation. Responsible for environmental monitoring (Viable) in liquid, lyophilized and dry powder manufacturing areas Responsible for preparation and implementation of SOP's Good Documentation recording and updation Responsible for Preparation and Implementation of SOP's. Viable monitoring in clean area of manufacturing and warehouse as per the defined schedule. Responsible for personnel monitoring. Responsible to participate in qualification, requalification, area qualification activities. Responsibilities other than defined in the JD are to be done as per instruction of HOD Qualifications Bachelor's Degree in Pharmacy, Microbiology, Biotechnology, Chemistry, or a related field. Master's Degree in Quality Assurance, Regulatory Affairs, or a related field (preferred but not mandatory). 3-5 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry. Hands-on experience with GMP inspections, environmental monitoring, and aseptic process simulations. Proven track record in sampling. Experience in reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Familiarity with SOP preparation and implementation. Involvement in change control, deviation management, and failure investigations. Show more Show less

Key Responsibilities JOB DESCRIPTION Business Development & Sales Execution Achieve and exceed sales targets for assigned oncology products. Develop and implement territory business plans to maximize growth. Identify and engage key decision-makers in hospitals, cancer centers, and other healthcare institutions. Ensure effective product promotion and awareness among oncologists, medical professionals, and key stakeholders. Key Account & Stakeholder Management Develop and maintain strong relationships with oncologists, healthcare providers, hospital administrators, and procurement teams. Provide scientific and commercial support to HCPs to drive brand adoption. Understand customer needs and tailor solutions to enhance patient outcomes. Market Intelligence & Competitor Analysis Stay updated on market trends, competitor activities, and regulatory changes. Gather insights from the field and provide feedback to the marketing and medical teams. Identify gaps and opportunities to improve product positioning. Cross-Functional Collaboration Work closely with the medical, marketing, and regulatory teams to ensure compliance and effective brand positioning. Support marketing initiatives and medical education programs. Collaborate with internal teams to ensure smooth product access and supply chain management. Compliance & Reporting Ensure adherence to company policies, industry regulations, and ethical standards. Maintain accurate and up-to-date records of sales activities, customer interactions, and market insights. Provide regular reports on sales performance, challenges, and strategic recommendations. Qualifications Qualifications & Experience: Bachelor's degree in Pharmacy, Life Sciences, or a related field; MBA preferred. 2+ years of experience in pharmaceutical sales, with a focus on oncology. Strong understanding of oncology therapies, treatment protocols, and market dynamics. Proven track record of achieving sales targets and building key customer relationships. Excellent communication, negotiation, and presentation skills. Ability to work independently and adapt to a dynamic environment. Key Competencies Business Acumen & Strategic Thinking Customer Relationship Management Market & Competitive Intelligence Strong Negotiation & Persuasion Skills Team Collaboration & Cross-Functional Coordination Ethical & Regulatory Compliance Awarenes Show more Show less

Amneal is coming in your city Hyderabad this 07th & 08th Jun 2025 for Walk In Drive Hiring for Projects & Engineering and Peptide expereince : Walk-In Interview Drive #Hyderabad We are coming to your city for a walk-in interview drive! If you're looking to build a rewarding career with a growing Global Pharmaceutical Company, dont miss this opportunity. Day 1: Saturday, 07th June 2025 Time: 9:00 AM to 5:00 PM Venue: Lemon Tree Premier Plot No. 2, Survey No. 64, HITEC City, Madhapur, Hyderabad 500081, Telangana Day 2: Sunday, 08th June 2025 Time: 9:00 AM to 5:00 PM Venue: Vivanta Hyderabad, Begumpet 1-10-147 & 148, Mayuri Marg, Begumpet, Hyderabad 500016, Telangana Opening in Engineering Department for the following opening : Designation : Sr Executive / Manager Yrs of Exp : 5-12 Yrs Qualification : M.Tech / B.E Expereince into Electrical : Experienced in electrical project execution, compliance, and commissioning, with strong knowledge of HT and LT electrical systems and a solid understanding of pharmaceutical equipment requirements. Expereince into Instrumentation Skilled in automation and instrumentation of equipment and utility systems, with hands-on experience in regulatory compliance, calibration, temperature mapping, and thermal validation. Expereince into Civil Civil engineer overseeing site execution, quality assurance, regulatory compliance, cross-functional coordination, and project documentation in pharmaceutical projects. Expereince into Mechanical Mechanical project scope includes HVAC systems, utility services, regulatory compliance, project timelines, and cross-functional coordination. In-depth knowledge of process equipment used in injectable pharmaceutical plants experience in the installation, commissioning, and qualification of water systems. Expereince into Process Strong expertise in equipment used for injectable manufacturing, with preferable knowledge of isolator systems. Experienced in the installation, commissioning, qualification, and documentation of process equipment Interested candidates who are unable to attend interview, can share their CV on below mentioned Email Id with subject line Application for Falcon indiacareers@amneal.com

Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements. Responsible for document management and preparation like BMR s, BPR s, master SOP s etc. Responsible for the handling of change control, deviations, CAPA, investigation etc. Responsible to give training to all the subordinates, technicians and operators of the department. Responsible for Audit and compliance on manufacturing shopfloor. Knowledge of kaizen and continuous improvements.

Responsible for document management like BMR s, BPR s, master SOP s etc. Responsible for preparation & review of the master documents of production. Responsible to ensure UAF working in area. Responsible for the handling of change control, deviations, investigation & CAPA, etc Responsible to give training to all the subordinates, technicians and operators of the department. Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HOD s instruction and guidance. Responsible for line clearance activity before commencing the operations. Responsible to check that all the records and logbooks related to aseptic manufacturing, vial filling and vial sealing machine. Responsible for preparation, review, revision, control and implementation of standard operating procedures of sterile manufacturing department. Responsible to ensure cleaning and sanitization of General, Controlled & Aseptic area. Inform immediately to department functional head for any observation/disturbance with respect to documents and machines found in area. Responsible for monitoring all the activities related to General, Control & Aseptic area. Responsible to ensure qualification and calibration status of equipment and instruments to avoid due/overdue. Responsible to ensure scheduled activity of respective area/equipment/instruments. Responsible to attend training as per schedule and to ensure training and work as per TNI. Follow the cGMP, Good Document Practice and discipline in the Company Premises.

Prepare the supply plan based on a rolling forecast to ensure timely availability of products. Place purchase orders (PO) to Contract Manufacturing Organizations (CMOs) in line with defined lead times. Coordinate with CMOs to achieve seamless supply execution and meet delivery objectives. Collaborate with the Sales team to address shortfalls and manage excess inventory effectively. Manage and monitor work orders within the ERP system to ensure alignment with production and supply plans. Analyze key MIS (Management Information Systems) reports to support data-driven decision-making across the supply chain. Graduation in any Field MBA is Preferable Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.

Prepare the supply plan based on a rolling forecast to ensure timely availability of products. Place purchase orders (PO) to Contract Manufacturing Organizations (CMOs) in line with defined lead times. Coordinate with CMOs to achieve seamless supply execution and meet delivery objectives. Collaborate with the Sales team to address shortfalls and manage excess inventory effectively. Manage and monitor work orders within the ERP system to ensure alignment with production and supply plans. Analyze key MIS (Management Information Systems) reports to support data-driven decision-making across the supply chain. Graduation in any Field MBA is Preferable Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.

Job Description Prepare the supply plan based on a rolling forecast to ensure timely availability of products. Place purchase orders (PO) to Contract Manufacturing Organizations (CMOs) in line with defined lead times. Coordinate with CMOs to achieve seamless supply execution and meet delivery objectives. Collaborate with the Sales team to address shortfalls and manage excess inventory effectively. Manage and monitor work orders within the ERP system to ensure alignment with production and supply plans. Analyze key MIS (Management Information Systems) reports to support data-driven decision-making across the supply chain. Qualifications Graduation in any Field MBA is Preferable About Us Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion. About The Team The Human Resources team partners with all aspects of the organization, driving success through the effective and innovative management of people for both current and future business needs. Key Roles That The Human Resources Team Performs Executive Role: Specialists in all aspects of people management. High-level input at strategic level into all key business decisions. Audit Role: Ensures all areas of the organization are compliant with legal requirements AND best practice employment policies and procedures. Facilitator Role: Close partnership to support, advise and extend the ability of all areas of the organization to meet their objectives through implementation of highly effective employment practices in areas such as Talent Acquisition, Learning and Development, Reward systems, Performance Management, Health and Wellbeing. Consultancy Role: Provide expert advice to the organization and it’s managers on any aspect of workforce management and employee relations and performance. Service Role: Ensure the organization is fully aware of and is equipped to deal with developments impacting employment matters, such as changes in legislation, changes in the characteristics of the labor market. Show more Show less

Job Responsibility JOB DESCRIPTION 1 Responsible for preparation of packaging planning on monthly and also daily as per the requirement and availability of materials. 2 Responsible to update on self-hygiene. 3 Responsible to attend the training as per training schedule and to ensure the training as per TNI. 4 Responsible to work as per standard operating procedures, in general area of sterile manufacturing department. 5 Responsible for preparation, review, revision, control and implementation of Standard Operating Procedures of General Area in Sterile Manufacturing Department. 6 Responsible for BPR Preparation. 7 Responsible to ensure that all equipments and lines are in validated and calibrated status. 8 Responsible to check that all the records and log books related to general area and equipment of packaging, inspection area. 9 Responsible to give training to all the subordinates, technicians and operators of the department. 10 To follow the cGMP, Good Document Practice and discipline in the department. 11 Responsible for document handling of Packing, and Inspection. 12 Responsible for monitoring of all the activities related to packing, and inspection. Qualifications Education: B.Sc., B.Pharma, M.Sc., M.Pharma Total Experience - 2 - 7 Year in sterile manufacturing plant Show more Show less

Job Description To handle and distribute various samples received for microbiological analysis. To maintain the logbook for the same. Maintain housekeeping of Microbiology lab. To maintain the inventory of various microbiological media, maintain log and status labels, media preparation, growth promotion test and reconciliation of media. Microbial culture handling and inoculum preparation. Water sampling and analysis of water samples as per schedule, with completion of all reports and records. Responsible for Sterility testing, Bacterial endotoxin testing, antibiotic microbial assay and bio burden testing of Raw material, in-process, finished products. Environmental monitoring of microbiology lab clean room area as per the defined schedule. Non-viable particle monitoring of microbiology lab clean room area as per the defined schedule. Responsible to identify and maintain data logging of EM Isolates. To perform disinfectant efficacy testing as per SOP. To perform microbial identification as per defined schedule. Responsible for handling and testing of biological indicator. To perform CCIT test of post media fill units. To perform observation of microbial plates exposed in manufacturing area. To perform media fill unit observation as per SOP. Responsible for reporting any OOS, Deviation to In-charge. Responsible for preparation of standard operating procedures of microbiology department. Responsible to co-ordinate with manufacturing, Engineering, and other QC personnel for respective Qualification / Validation / Re-qualification activity for timely completion of activities. Responsible to participate in perform qualification activities of manufacturing and Microbiology area. Responsible for Compressed air /nitrogen gas monitoring and Personnel monitoring Preparation of indents as per the materials/product requirements. To initiate and review of a) Change controls b) Out of specifications c) Deviations. To attain and complete self- training record. Preparation of study protocols with respect to laboratory. Review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Preparation of COA. To keep neat and cleanliness at workplace and follow the good laboratory practices and safety related instruction in the laboratory. To perform water analysis and maintain daily water trend. Sampling, testing and release of Raw material, packing material, miscellaneous material samples and in process sample and maintain reserve sample as per SOP. To keep update of instruments logbooks and to record the data in Laboratory Notebook / and respective software. To monitor and plan the activities of various glassware and items required for microbiological analysis with respect to their cleaning, sterilization, and dehydrogenation. To maintain log and status labels for all such items and reconciliation record. Responsible for Pure culture handling and maintenance. To maintain daily logs of area with respect to temperature, humidity, differential pressure, area cleaning, disinfectant preparation, etc.. To record such reading in the respective records and logs. Qualifications B.Sc. / M.Sc. Show more Show less

Maintain up-to-date launch trackers (covering OSD, Injectable, Ophthalmic, and CMO projects) Coordinate with India cross-functional teams (CFTs) Manage the introduction of new product forms and trade dress readiness Attend NPL meetings and sharing minutes of meetings (MoMs) Prepare presentations for tracking and reporting purposes Coordinate for JDE set up process, COGS calculation, and serialization activities Follow up on all action items from the meetings and ensure all action items are closed in a timely manner Provide real-time updates on API, materials, and packaging component status Track manufacturing, packaging, and release status for NPLs Follow up on stability sample delivery, chamber charging, and analysis for site transfer projects Collaborate with Regulatory Affairs on CBE-30 and PAS filing documents Communicate across all stakeholders and upper management to inform on the project status, critical path items, risks, and delays, if timeline does not meet Complete transport request forms for upcoming launches and track the shipment Good communication and negotiation skills

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible to perform the environment monitoring activities Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring eg, plates, samplers, swabs etc. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material eg, plates, swabs, etc. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record.

Prepare the supply plan based on a rolling forecast to ensure timely availability of products. Place purchase orders (PO) to Contract Manufacturing Organizations (CMOs) in line with defined lead times. Coordinate with CMOs to achieve seamless supply execution and meet delivery objectives. Collaborate with the Sales team to address shortfalls and manage excess inventory effectively. Manage and monitor work orders within the ERP system to ensure alignment with production and supply plans. Analyze key MIS (Management Information Systems) reports to support data-driven decision-making across the supply chain.

Amneal Pharmaceuticals is looking for Officer, Process Development to join our dynamic team and embark on a rewarding career journey Develop and optimize manufacturing processes Support trials, validation, and scale-up activities Analyze data to improve yield and efficiency Ensure compliance with regulatory standards

Amneal Pharmaceuticals is looking for Senior Officer, Capsulation to join our dynamic team and embark on a rewarding career journey The Senior Officer plays a crucial role in the organization, responsible for overseeing and executing various tasks and projects to ensure the smooth functioning of operations This role requires strong leadership, analytical skills, and the ability to collaborate effectively with team members and stakeholders Key Responsibilities: Leadership:Provide leadership and guidance to team members, fostering a positive work environment Lead by example, demonstrating professionalism, integrity, and dedication to the organization's goals and values Project Management:Manage and coordinate projects from initiation to completion, ensuring adherence to timelines and budget constraints Develop project plans, allocate resources, and monitor progress to achieve project objectives Identify and mitigate risks to project success, implementing appropriate solutions as needed Operational Efficiency:Streamline processes and procedures to improve operational efficiency and effectiveness Identify opportunities for automation or technological enhancements to optimize workflow and productivity Collaborate with cross-functional teams to implement process improvements and best practices Data Analysis and Reporting:Analyze data to identify trends, patterns, and insights relevant to the organization's objectives Generate reports and presentations to communicate findings and recommendations to key stakeholders Utilize data-driven insights to inform decision-making and drive continuous improvement initiatives Stakeholder Engagement:Build and maintain relationships with internal and external stakeholders, including clients, partners, and vendors Collaborate with stakeholders to understand their needs and requirements, ensuring alignment with organizational objectives Effectively communicate project updates, issues, and resolutions to stakeholders, fostering transparency and trust Compliance and Risk Management:Ensure compliance with relevant laws, regulations, and internal policies and procedures Proactively identify and address potential risks and compliance issues, implementing appropriate controls and safeguards Keep abreast of industry developments and best practices to inform risk management strategies

Amneal Pharmaceuticals is looking for Assistant, Packing to join our dynamic team and embark on a rewarding career journey Pack products as per standards and instructions Label and organize packages for shipment Check for damages and quality issues Maintain cleanliness in the packing area

Amneal Pharmaceuticals is looking for Senior Assistant to join our dynamic team and embark on a rewarding career journey Assist in administrative and operational duties Manage documentation and record keeping Coordinate internal communication and schedules Support managers in daily office functions

Job Description Product evaluation, identification, therapy area and competition mapping Prepare business cases models with customization of strengths, In-house, In-licensing, partnership with agreed terms and conditions of the business opportunities Product Valuations of current and potential new opportunities with discounting techniques i.e., DCF, NPV, IRR, PBP, ROI etc. Financial Modeling to check all possible financial viability of the project (Revenue, Sales, COGS, EBITDA, CAPEX, Gross Margin etc.) Build detailed Business cases, strategy document for all selected products Generate competitive intelligence data for peers, partners, products, and market Supporting team in analyzing the various new business opportunities. Building ROI for Investment required for facility and product acquisition OR CAPEX justifications Preparation and compilation of power point presentations and Ad-hoc reports Automation on reports and templates including large volume IQVIA data Update of Master Portfolio and supporting in data requirements Market research of products to identify and track competition, Sales, and Volume and to check the lucrativeness of the products Improvise and support team in presentation of various data requirements to the stakeholders Escalate issues that weaken portfolio and project success Required skills and qualifications B Pharma and qualification of MBA in Finance would be preferred Overall experience of 5 to 7 years and Preferably 3 + years of functional experience in generic Portfolio Management Exhibit strong knowledge of the Pharmaceutical domain with a comprehensive understanding of the US & EU Pharma market Must understand pharmaceutical business process such as Product Development, Dossier Filing and Pharma Market Good understanding and hands-on experience of using various analytical tools and databases Good presentation skills and ability to independently conduct secondary research Good communication, networking, and interpersonal skills to connect with internal and external stakeholders Ambitious and Self-driven Advanced expertise in MS Excel, MS Word, MS PowerPoint Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.

A m

Job Description Currently we are having Opening in ARD Department, below is the JD of position. Handling of instrument like HPLC, GC, GC-MSMS, LC-MSMS etc. Knowledge about regulatory requirement for Extractable and Leachable Analytical method development, Method verification and validation for analytical method. Preparation and review of all methods, verification/validation protocols and reports. Operation, maintenance, troubleshooting and calibration of analytical equipment. Qualifications M.Pharm (QA/ Med.Chemistry) / M.Sc. (Analytical or Organic chemistry) About Us Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion. About The Team The Human Resources team partners with all aspects of the organization, driving success through the effective and innovative management of people for both current and future business needs. Key Roles That The Human Resources Team Performs Executive Role: Specialists in all aspects of people management. High-level input at strategic level into all key business decisions. Audit Role: Ensures all areas of the organization are compliant with legal requirements AND best practice employment policies and procedures. Facilitator Role: Close partnership to support, advise and extend the ability of all areas of the organization to meet their objectives through implementation of highly effective employment practices in areas such as Talent Acquisition, Learning and Development, Reward systems, Performance Management, Health and Wellbeing. Consultancy Role: Provide expert advice to the organization and it’s managers on any aspect of workforce management and employee relations and performance. Service Role: Ensure the organization is fully aware of and is equipped to deal with developments impacting employment matters, such as changes in legislation, changes in the characteristics of the labor market. Show more Show less